Bredlich R O, Stracke S, Gall H, Proebstle T M
Abteilung Dermatologie, Universität Ulm.
Dtsch Med Wochenschr. 1997 Mar 14;122(11):328-32. doi: 10.1055/s-2008-1047617.
A 52-year-old man had been in terminal renal failure for 6 years. On haemodialysis under heparin without complications, acral skin necroses occurred. Even with low-molecular heparin anticoagulation further lesions developed. Within 12 weeks of haemodialysis being performed without heparin the necroses healed, but they recurred when heparin was again added for dialysis. On admission the patient was in poor general condition, with a weight of 55 kg (height 175 cm). LABORATORY INVESTIGATIONS: The heparin-induced platelet aggregation (HIPA) test was positive in the absence of thrombocytopenia. Na-heparin reacted positively in three out of four tests, but Danaparoid did not react.
The skin necroses once again healed after the heparinoid Danaparoid, which had not reacted in the HIPA test, had been substituted for heparin.
This case illustrates that skin necroses, thrombocytopenia and thromboembolism can be independent signs of immunologically induced platelet aggregation.
一名52岁男性终末期肾衰竭已6年。在肝素抗凝下进行血液透析无并发症,但出现了肢端皮肤坏死。即使使用低分子肝素抗凝,仍有进一步的病变出现。在无肝素进行血液透析的12周内,坏死愈合,但再次添加肝素进行透析时又复发。入院时患者一般状况较差,体重55千克(身高175厘米)。实验室检查:在无血小板减少的情况下,肝素诱导的血小板聚集(HIPA)试验呈阳性。4次试验中有3次钠肝素反应阳性,但达那肝素无反应。
在HIPA试验中无反应的类肝素达那肝素替代肝素后,皮肤坏死再次愈合。
该病例表明,皮肤坏死、血小板减少和血栓栓塞可能是免疫诱导血小板聚集的独立征象。